Bringing Tomorrow's Treatments to the Modern Day
Frequently Asked Questions
What is Clinical Research?
Clinical research involves conducting scientific studies with human participants to examine the safety, efficacy, and effectiveness of medical interventions, treatments, or therapies. Its primary goal is to produce valuable evidence that informs medical decision-making, enhances medical knowledge, and enhances patient care.
Can you provide information on the various categories of clinical research studies?
Clinical research encompasses various research methodologies such as clinical trials, observational studies, andological studies. Clinical trials are conducted in phases (Phase 1, 2, 3, and sometimes Phase 4) to evaluate the safety, dosage, effectiveness, and side effects of a medical intervention.
Who takes part in Clinical Research?
Clinical research requires the involvement of individuals who satisfy certain criteria, which may include patients with a specific medical condition or healthy volunteers. Depending on the study's goals and target population, participants may differ in age, gender, health status, and other factors.
Is there any compensation for taking part in a Clinical Trial?
All participants in the clinical trial are remunerated for their time and travel expenses.
Can my insurance be charged for taking part in a Clinical Trial?
The pharmaceutical company will cover all study procedures, and you and your insurance will not incur any costs.
Is it possible for me to exit a clinical research study?
Participants in a clinical research study are entitled to withdraw from the study at any point without having to provide an explanation. The participant's decision will be respected by the researchers and study coordinators, who will also ensure their continued safety and care.
Can individuals choose to participate in clinical research on their own accord?
Participation in clinical research is completely optional. People can decide whether or not to take part a study by reviewing the study information, weighing the potential risks and benefits, and seeking advice from healthcare professionals or loved ones.
Can you describe what I might go through during a clinical trial?
In a clinical trial, your health will be monitored by the study team. Being a part of a clinical trial may require more time and involve additional tests and treatments compared to standard treatment. Additionally, the study team may request you to maintain symptom log, fill out forms about your well-being, or perform other tasks
What measures are taken to ensure the safety of in clinical research?
The process of informed consent protects participants in clinical research by ensuring that they fully understand the study's purpose, procedures, potential risks, and benefits before deciding to participate Moreover, research studies must comply with ethical guidelines, obtain approval from research ethics committees, and adhere to regulatory requirements to safeguard participant safety, privacy, and rights.
In case I don't have any means of transportation, what should I do?
You don't have to worry as we provide free transportation services for both pick-ups and drop-offs.
Is there any danger involved in taking part in clinical studies?
Although clinical research studies may carry some risks, such as potential side effects from experimental treatments or procedures, researchers take extensive precautions to minimize these risks and closely monitor participants throughout the study. To help participants make an informed decision, the potential benefits and risks of a study should be thoroughly explained during the informed consent process.
How can I determine my eligibility for a clinical trial?
Clinical trials are open to individuals of various ages, ethnicities, and racial. To participate in a specific clinical trial, you must meet the eligibility requirements. Eligibility is typically determined through a screening visit, and all trials have inclusion and exclusion criteria.